Associated Papers
Catalyzing precision: unraveling the diagnostic conundrum of tunisian familial hypophosphatasia case through integrative clinical and molecular approaches.
Amri Y et al.
Molecular Genetics and Genomics : Mgg, 2024
Clinical and genetic characteristics of hypophosphatasia in Chinese children.
Liu M et al.
Orphanet Journal of Rare Diseases, 2021
Lethal perinatal hypophosphatasia caused by a novel compound heterozygous mutation: a case report.
Yu F et al.
Bmc Pediatrics, 2019
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